BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    90-0322 VAGINAL DELIVERY TRACEPAK

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code KDD·December 7, 2001

    90-0322 VAGINAL DELIVERY TRACEPAK

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code KDD·December 7, 2001

    90-0322 VAGINAL DELIVERY TRACEPAK

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code KDD·December 7, 2001

    90-0322 VAGINAL DELIVERY TRACEPAK

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIEES, INC.·Product code KDD·December 7, 2001

    SIGMA PS CEM FEM SZ5 R

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS 121965·Product code JWH·June 27, 2014

    ACCLAIM ENCORE 2.25

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·October 25, 2010

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·January 7, 2013

    SMR GLENOSPHERE Ø 40MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·December 15, 2021